[0001] The present invention relates to an improved non-aqueous, built liquid detergent
composition.
[0002] Non-aqueous, built liquid detergent compositions have already been proposed in the
art. Thus, US Patents 2,864,770, 2,940,938 and UK Patent 1,008,016 describe non-aqueous,
built liquid detergent compositions, comprising a colloidal suspension of a polyphosphate
builder salt in a liquid vehicle, which may be a nonionic detergent or a short-chain
glycol. These prior proposals require careful processing, and require very fine polyphosphate
builder salts.
[0003] U.K. Patents 1,205,711, 1,270,040 and 1,292,352 describe substantially non-aqueous,
built liquid detergent compositions in which the builder salts are suspended in a
liquid medium by means of an inorganic, highly voluminous carrier material. These
compositions however show either an undesirable syneresis, or are not sufficiently
pourable for practical purposes.
[0004] Another prior proposal, US Patent 3,368,977, describes a non-aqueous built liquid
detergent composition, comprising an anionic detersive surfactant, a solvent for the
surfactant, and a phosphate builder salt in suspension in the liquid. The surfactant
must be soluble in the solvent, which restricts the choice thereof, and the phosphate
builder salt should be of a very finely divided type, as otherwise qo stable suspensions
are obtained.
[0005] In addition, UK Patent 1,370,377 discloses a non-aqueous liquid detergent composition,
comprising a solid particulate water-soluble salt dispersed in a liquid medium, an
anionic surface-active agent and a suspending agent. The particle size of the inorganic
salt should be such that it can act as an abrasive. The suspending agent confers Bingham
plastic character to the composition, and is for example a highly voluminous inorganic
carrier material as in UK Patent 1,205,711.
[0006] Again the storage stability of these compositions does not seem to be satisfactory
for many practical purposes, a period of two weeks being mentioned in this patent.
[0007] Finally, German Patent Application 2,233,771, laid open to public inspection on 1st
February 1973, describes non-aqueous built liquid detergent compositions comprising
a bleaching agent, a builder salt, a liquid detergent and a polyol or an ether of
a polyol as solvent. Again this composition requires a very fine division of the solid
material therein, and the products obtained are very viscous indeed, in fact paste-like.
[0008] Therefore, in the prior art there has been no lack of proposals for non-aqueous built
liquid detergent compositions, but so far no generally satisfactory compositions have
been proposed.
[0009] The present invention has as an object to overcome and/or significantly reduce the
drawbacks of these prior proposals.
[0010] It has been found that this object, and others, can be achieved by using a specific
type of suspension stabilizer in a non-aqueous, solvent-containing medium.
[0011] Indeed, it has been found that the use of an at least partially hydrolyzed copolymer
of maleic anhydride with ethylene or vinylmethylether in a non-aqueous, solvent-containing
liquid medium, in the presence of a strongly alkaline material, provides for a liquid
medium in which builder salts can be stably suspended. These compositions show a storage
stability of 2% or less phase separation per month.
[0012] In essence therefore, the present invention relates to a substantially non-aqueous,
built liquid detergent composition comprising as essential ingredients:
1) a surface-active detergent material
2) a solvent
3) an at least partially hydrolyzed copolymer of maleic anhydride with ethylene or
vinylmethylether
4) a strongly alkaline material, and
5) a builder salt, and, if necessary,
6) a buffer.
[0013] These essential ingredients will be discussed below in more detail.
The surface-active detergent material
[0014] It is essential that the surface-active material is either liquid at room temperature,
or liquefiable at room temperature, e.g. by forming a solution with the solvent. Bearing
these requirements in mind, suitable surface-active detergents may be found in the
classes of soaps and non-soap detergents, e.g. the anionic, cationic, amphoteric,
zwitterionic and nonionic detergent surfactants, or mixtures thereof.
[0015] A preferred group of suitable detergent surfactants is the group of nonionic surfactants.
Nonionic detergent surfactants are well known in the art. They normally consist of
a water-solubilizing polyoxyalkylene group in chemical combination with an organic
hydrophobic group derived, for example, from alkylphenols in which the alkyl group
contains from about 6 to about 12 carbon atoms, dialkylphenols in which each alkyl
group contains from 6 to 12 carbon atoms, primary, secondary or tertiary aliphatic
alcohols having from 8 to 20 carbon atoms, monocarboxylic acids having from 10 to
about 24 carbon atoms in the alkyl group, polyoxypropylene, fatty acid mono- and di-
alkylolamides in which the alkyl group of the fatty acid radical contains from 10
to about 20 carbon atoms and the alkylol group is a lower alkylol group having from
1 to 3 carbon atoms, and ethoxylated derivatives thereof, for example tallow fatty
acid amide condensed with 20 moles of ethylene oxide. The nonionic detergent surfactants
normally have molecular weights of from about 300 to about 11,000.
[0016] Mixtures of different nonionic detergent surfactants may also be used. Mixtures of
nonionic detergent surfactants with other detergent surfactants such as anionic, cationic
and ampholytic detergent surfactants and soaps may also be used, but again such mixtures
must be liquid or liquefiable at room temperatures.
[0017] Especially preferred are those nonionics in which the organic hydrophobic group contains
both ethylene oxide and propylene oxide moieties. Typical examples thereof are primary
C
13-C
15 alcohols, condensed with 7-9 moles of ethylene oxide plus propylene oxide, the alkylene
oxides being used in a weight ratio of e.g. 92:8.
[0018] The amount of the surface-active detergent material, present in the composition,
is generally from 5 to 45%, preferably from 8 to 20%, and particularly preferably
from 10 to 12%.
The solvent
[0019] The solvent is also critical, in that the at least partially hydrolyzed copolymer
should be soluble therein. Basically, those solvents can be used in which the at least
partially hydrolyzed copolymer under the following standard conditions shows a solubility
of at least 1.5% by weight, after having been dissolved at about 80°C in the solvent
until a clear solution is obtained. The solvent molecules should bear at least one
hydroxyl group.
[0020] Although not critical, it is beneficial to use those solvents in which also, in case
solid or liquefiable surface-active detergents are used, the latter can be dissolved.
[0021] Typical examples of suitable solvents, meeting the above requirement with regard
to the at least partially hydrolyzed copolymer, are triethyleneglycol monoethylether,
ethyleneglycol monoethylether, ethyleneglycol mono-n-butylether, diethyleneglycol
monomethylether, diethyleneglycol monoethylether, diethyleneglycol mono-n-butylether,
4-hydroxy-4-methyl-2-pentanone, and polyethyleneglycols with an average molecular
weight of 200-3,000. Mixtures of these solvents can also be used. The above-specified
ether-type solvents are preferred, of which triethyleneglycol monoethylether is the
preferred representative. Ethanol can also be used, but only in conjunction with one
of the above solvents.
[0022] The solvent is generally present in the composition in an amount of from 5 to 60%,
preferably from 25 to 35%, and particularly from 28 to 32%. The weight ratio of solvent
to surface-active detergent material may vary widely, but in order to obtain compositions
which can easily be dispensed, the ratio is preferably from 3:1 to 1:1.
The copolymer
[0023] The copolymer is an at least partially hydrolyzed hydrolyzable copolymer of maleic
anhydride with ethylene or vinylmethylether. These hydrolyzable copolymers as such
are well known in the art; they are described, for instance, in US Patent 3,328,309.
[0024] It is essential that these copolymers are used in an at least partially hydrolyzed
form. The copolymer must be hydrolyzed for at least 300AI and preferably for about
50%, whereby the percentage is based upon the total number of maleic anhydride groups
originally present in the copolymer. The copolymer may also be completely hydrolyzed.
The at least partially hydrolyzed copolymer is generally present in an amount of from
0.1 to 1.0%, preferably from 0.25 to 0.7%, and particularly from 0.2 to 0.4%.
The strongly alkaline material
[0025] Essential for the role of the at least partially hydrolyzed copolymer as stabilizer
in the composition of the invention is the presence of a strongly alkaline material
in a finely divided form in the composition. The mean particle size of this material
should be less than 50 micrometers. The strongly alkaline material to be used in the
present invention is one wnich, when dissolved in distilled water at 20°C, at a concentration
of 1% by weight, yields a pH of >10. Suitable examples of inorganic materials are
sodium(di)silicate, sodium hydroxide, sodium carbonate, sodium sesquicarbonate, and
trisodium orthophosphate, and suitable examples of organic materials are ethylene
diamine, hexamethylene diamine, diethylamine and propylamine. The strongly alkaline
material may also act as a buffer in the system; if it does not provide for a sufficient
buffering capacity, an additional buffer, such as borates, may be added.
[0026] In general, the strongly alkaline material is present in the composition in an amount
of from 2.5 to 20%, preferably from 5 to 15%, and particularly from 11 to 13%.
The builder salt
[0027] The builder salt in the present invention may be any suitable organic and/or inorganic
builder salt. Typical examples thereof are the alkali metal ortho-, pyro-, meta- and
tripolyphosphates, alkali metal carbonates, -silicates, sodium aluminosilicates (zeolites),
sodium carboxymethyloxy succinate, sodium carboxymethyloxy malonate, sodium citrate,
salts of amino polycarboxylic acids such as NTA, etc. In general, these builder salts
are present in an amount of from 1 to 70%, preferably from 10 to 60%, and particularly
from 20 to 50%.
[0028] The compositions of the invention may furthermore contain ingredients commonly incorporated
in liquid detergents, such as bleaching agents, bleach activators, hydrotropes, enzymes,
enzyme-stabilizing agents, fluorescers, soil-suspending agents, anti-soil redeposition
agents, perfumes, bactericides, corrosion inhibitors, foam boosters, foam depressors,
(co)solvents not containing a hydroxyl group, softening agents, all without substantially
modifying the fundamental characteristics of the composition of the invention.
[0029] In this respect it is of advantage that all suspended particles are of a size less
than 50 micrometers.
[0030] It has also been found that the addition of certain other polymers can further improve
the stability of the final composition. Typical examples of such polymers are polyethylene
oxide waxes (MW up to a few million; viscosity 2,000-4,000 cP at 1% conc.) and hydroxypropylcellulose
(viscosity 5% aqueous solution 150-400 cP (Brookfield LVF). These polymers can be
present in an amount of from 0.05 to 0.7%, preferably from 0.1 to 0.4%.
[0031] The compositions of the present invention can be made by any suitable mixing process.
It is, however, an essential process condition that the at least partially hydrolyzed
copolymer is dissolved in the solvent at about 80
0C to a clear solution before any of the other components are added. To the solution
thus obtained, the detergent-active material can be added, and subsequently the strongly
alkaline material under thorough agitation. If the at least partially hydrolyzed copolymers
are not available as such, they must be prepared prior to admixture with the other
ingredients. This can be done separately by, for example, spraying the required amount
of water on the anhydrous copolymer in its anhydride form in a suitable mixing vessel.
[0032] The present invention will further be illustrated by way of example.
[0033] If a completely hydrolyzed copolymer is used, it is dissolved in the solvent and
kept at about 80°C until the [H
+] (in mg eq/g solution) is from 0.79-0.88, preferably from 0.82-0.84 (measured as
a 10% by weight solution in triethyleneglycol monoethylether).

These examples show the criticality of the lower degree of hydrolysis of the copolymer.
[0034] ,Replacing the copolymer with the specific viscosity of 0.1-0.5 by the same copolymers,
but with specific viscosities of 1.0-1.4, 1.5-2.0 and 2.6-3.5 give analogous results.

[0035] The nonionic detergent was varied in these products as follows, and the following
percentages phase separation were measured:

1. A non-aqueous, built liquid detergent composition, essentially comprising:
a) from 5-45% by weight of a surface-active detergent material which is liquid or
liquefiable at room temperature;
b) from 0.1-1% by weight of an at least for 30% hydrolyzed, hydrolyzable copolymer
of maleic anhydride with ethylene or vinylmethylether;
c) from 5-60% by weight of a hydroxyl group-containing solvent, in which the at least
partially hydrolyzed copolymer (b) shows a solubility of at least 1.5% by weight after
having been dissolved at about 80°C until a clear solution is obtained;
d) from 2.5-20% by weight of a strongly alkaline material having a mean particle size
of less than 50 micrometers, and yielding a pH (1% by weight aqueous solution at 20°C)
of equal to or higher than 10;
e) from 1-70% by weight of an organic and/or inorganic builder salt.
2. A composition according to claim 1, essentially comprising
from 8-20% by weight of a)
from 0.25-0.7% by weight of b)
from 25-35% by weight of c)
from 5-15% by weight of d), and
from 10-60% by weight of e).
3. A composition according to claim 2, essentially comprising
from 10-12% by weight of a)
from 0.2-0.4% by weight of b)
from 28-32% by weight of c)
from 11-13% by weight of d), and
from 20-50% by weight of e).
4. A composition according to claim 1, further comprising from 0.05-0.7% by weight
of a polymer selected from the group consisting of polyethylene oxide waxes with a
molecular weight of up to a few million, and a viscosity of 2,000-4,000 cP in a 1%
aqueous solution (250C), and hydroxypropylcellulose with a viscosity of 150-400 cP (Brookfield LVF in a
5% aqueous solution at 250C).
5. A composition according to claim 4, comprising from 0.1-0.4% by weight of the polymer.
6. A composition according to claim 1, wherein the surface-active detergent material
is a nonionic surface-active agent, the copolymer is hydrolyzed for at least 50%,
the solvent is triethyleneglycol monoethylether, the strongly alkaline material is
sodium disilicate and the builder salt is sodium tripolyphosphate.
7. A process for making a composition according to claim 1, in which first the partially
hydrolyzed copolymer is dissolved in the solvent at 80°C until a clear solution is
obtained, after which the other components are added.
8. A process for making a composition according to claim 1, in which first the completely
hydrolyzed copolymer is dissolved in the solvent at 80°C until the [H+] of the resulting solution is from 0.79-0.88, especially 0.82-0.84 mg eq/g solution
(measured as a 10% by weight solution in triethyleneglycol monoethylether), after
which the other components are added.